Ms Louise Rawcliffe BSc MBA

Louise has over 20 years’ experience in the pharmaceutical industry within regulatory affairs and regulatory compliance.
She has considerable knowledge of EU/US clinical trial regulations as well as medical device licensing procedures and regulations, directives and guidelines.
She has experience in managing compliance programmes for global clinical trials.
Louise has facilitated regulatory authority inspections of both UK- and US-based investigator sites and GMP and device manufacturing facilities.
Her extensive experience covers all phases of clinical development.
Louise also has 10 years’ experience in pharmacovigilance for licensed and investigational medicinal products.